Canonical Allele Identifier: PA2828000671
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 83212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile547Val
CA006325
NM_001354902.2:c.1639A>G